Sulfaperin

Base Information

• Chemical Name: Sulfaperin
• CAS No.: 599-88-2
• Molecular Formula: C11H12 N4 O2 S
• Molecular Weight: 264.308
• European Community (EC) Number: 209-976-4
• UNII: W5E840UV9P
• DSSTox Substance ID: DTXSID2057782
• Nikkaji Number: J9.442K
• Wikipedia: Sulfaperin
• Wikidata: Q6577298
• NCI Thesaurus Code: C72854
• Metabolomics Workbench ID: 144393
• ChEMBL ID: CHEMBL2105499
• Mol file: 599-88-2.mol

Synonyms:isosulfamerazine;sulfaperine;sulfene

Chemical Property of Sulfaperin

Chemical Property:

• Vapor Pressure: 7.03E-11mmHg at 25°C
• Melting Point: 262-263°
• Boiling Point: 519.1°Cat760mmHg
• Flash Point: 267.8°C
• PSA: 106.35000
• Density: 1.439g/cm³
• LogP: 2.90300
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 264.06809681
• Heavy Atom Count: 18
• Complexity: 352

Purity/Quality:

99% ^*data from raw suppliers

4-Amino-N-(5-methylpyrimidin-2-yl)benzenesulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CN=C(N=C1)NS(=O)(=O)C2=CC=C(C=C2)N

Technology Process of Sulfaperin

There total 4 articles about Sulfaperin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-acetyl-sulfanilic acid-(5-methyl-pyrimidin-2-ylamide) (21415-17-8) → sulfaperin (599-88-2)

Guidance literature:

With sodium hydroxide;

DOI:10.1021/ja01856a046

Reference yield:

5-methylpyrimidin-2-amine (50840-23-8) → sulfaperin (599-88-2)

Guidance literature:

Multi-step reaction with 2 steps

2: aq. NaOH solution

With sodium hydroxide;

DOI:10.1021/ja01856a046

Reference yield:

p-acetylaminobenzenesulfonyl chloride (121-60-8) → sulfaperin (599-88-2)

Guidance literature:

Multi-step reaction with 2 steps

2: aq. NaOH solution

With sodium hydroxide;

DOI:10.1021/ja01856a046

upstream raw materials:

N-acetyl-sulfanilic acid-(5-methyl-pyrimidin-2-ylamide)

5-methylpyrimidin-2-amine

p-acetylaminobenzenesulfonyl chloride